Job Summary:

Laboratory position which involves development and validation of analytical methodology in support of the research projects involving testing of pharmaceutical components and/or drug products. Under general supervision, the position may require proficiency in support formulation, development method improvement and validation, testing per compendial pharmacopeia, etc.

Job Responsibilities

• Proficiency in multiple instrumentation techniques such as HPLC, GC, UV-VIS, dissolution equipment, pH measurement, titration, etc.
• General knowledge of cGMP and FDA requirements.
• Perform stability testing for GMP and R&D finished products
• Conduct analytical testing of API, excipients and components following compedial and validated methods
• Perform analytical method validation and method transfer with a minimum supervision.
• Follow company’s SOPs, STPS and comply with safety regulations.
• Maintain detailed record of experiments in the laboratory notebook.
• Timely communicate to supervisor(s) the obtained data and any issues aroused during testing
• Ability to analyze and interpret the analytical data under minimum supervision.
• Interpret specifications, standard operating procedures, and standard testing procedures.
• Writes/reviews protocols, reports, SOPs and STPs applicable to analytical laboratory under the supervision.
• Works as a member of a team to achieve all outcomes
• Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements.
• Performs all work in support of our Values: Collaboration, Courage, Perseverance, and Passion
• All other relevant duties as assigned